Department of Preventive Medicine and Public Health, University of Granada, Granada, Spain.
Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
Prostate Cancer Prostatic Dis. 2022 Sep;25(3):411-421. doi: 10.1038/s41391-021-00481-7. Epub 2022 Jan 6.
The association of obesity with biochemical recurrence (BCR) after treatment of clinically localised prostate cancer (PC) shows inconsistent results. Our aim was to systematically review all evidence evaluating obesity as a prognostic factor for BCR.
We searched PubMed, Web of Science and Scopus, from inception to June 1, 2021. Cohort studies reporting BCR among PC patients stratified by body mass index (BMI) were included. To assess the quality of the selected studies, we used the Newcastle-Ottawa scale (NOS). Risk of BCR among obese patients (BMI ≥ 30 kg/m) was compared with normal weight (BMI < 25), pooling individual hazard ratios (HR) in random-effect meta-analysis. Associations for continuous BMI per 5 kg/m were also calculated. Subgroup analyses were conducted to assess reasons for heterogeneity and causal criteria were formally evaluated.
We identified 46 cohort studies including 86,490 PC patients. A total of 14,719 (17.1%) patients developed BCR. There was no consistent definition of BCR. Obesity was associated with BCR (HR: 1.25, 95% CI: 1.11-1.39, I: 70.3%), and there was a 10% increase (95% CI: 4-15%, I: 66.3%) in BCR per 5 kg/m increase in BMI. The heterogeneity was high but decreased in the subgroup of highest-quality NOS score and when the BMI was measured by the researchers (I: 0.0%). The association was consistent in patients receiving radical prostatectomy but not in patients receiving other therapies.
Obesity showed a moderate, consistent relationship with biochemical recurrence after radical prostatectomy. Measurement of BMI and BCR was variable, highlighting the need for standardised clinical guidelines. Preventive weight control programs may have a role in reducing BCR for clinically localised PC patients.
肥胖与接受局限性前列腺癌(PC)治疗后的生化复发(BCR)之间的关联结果不一致。我们的目的是系统地回顾所有评估肥胖作为 BCR 预后因素的证据。
我们检索了 PubMed、Web of Science 和 Scopus,从创建到 2021 年 6 月 1 日。纳入了报告按体重指数(BMI)分层的 PC 患者中 BCR 的队列研究。为了评估所选研究的质量,我们使用了纽卡斯尔-渥太华量表(NOS)。肥胖患者(BMI≥30kg/m)与正常体重(BMI<25kg/m)相比,BCR 风险采用随机效应荟萃分析计算个体风险比(HR)。还计算了 BMI 每增加 5kg/m 的连续 HR。进行了亚组分析以评估异质性的原因,并正式评估因果标准。
我们确定了 46 项队列研究,包括 86490 名 PC 患者。共有 14719 名(17.1%)患者发生 BCR。BCR 没有一致的定义。肥胖与 BCR 相关(HR:1.25,95%CI:1.11-1.39,I:70.3%),BMI 每增加 5kg/m,BCR 增加 10%(95%CI:4-15%,I:66.3%)。异质性很高,但在 NOS 评分最高的亚组和研究人员测量 BMI 时降低(I:0.0%)。该关联在接受根治性前列腺切除术的患者中是一致的,但在接受其他治疗的患者中则不一致。
肥胖与根治性前列腺切除术后生化复发有中度、一致的关系。BMI 和 BCR 的测量存在差异,这突出了制定标准化临床指南的必要性。对临床局限性 PC 患者进行预防性体重控制可能有助于降低 BCR。